Canonical Allele Identifier: CA399605371
Gene: MLX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42571602G>T , CM000679.2:g.42571602G>T GRCh38
NC_000017.10:g.40723620G>T , CM000679.1:g.40723620G>T GRCh37
NC_000017.9:g.37977146G>T NCBI36
NG_029442.1:g.9543G>T
NG_031960.1:g.11230C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000435881.7:c.734G>T MANE Select ENSP00000416627.1:p.Ter245Leu
ENST00000246912.8:c.896G>T ENSP00000246912.3:p.Ter299Leu
ENST00000346833.8:c.644G>T ENSP00000320913.3:p.Ter215Leu
ENST00000435881.6:c.734G>T ENSP00000416627.1:p.Ter245Leu
ENST00000585403.5:n.941G>T
ENST00000588320.1:n.1210G>T
ENST00000590050.5:n.900G>T
NM_170607.2:c.896G>T NP_733752.1:p.Ter299Leu
NM_198204.1:c.734G>T NP_937847.1:p.Ter245Leu
NM_198205.1:c.644G>T NP_937848.1:p.Ter215Leu
NM_198204.2:c.734G>T MANE Select NP_937847.1:p.Ter245Leu
NM_170607.3:c.896G>T NP_733752.1:p.Ter299Leu
NM_198205.2:c.644G>T NP_937848.1:p.Ter215Leu